Supporting Treatment for Opioids and Recovery Capital (STORC) - R61 Phase

Part of paid clinical trials in Philadelphia, Pennsylvania.

Sponsor
Friends Research Institute, Inc.
Study ID
NCT07787039
Status
Not Yet Recruiting

Notify me when recruiting opens

Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.

Not yet recruiting

Add your contact details and location so we can keep your interest tied to this study.

Conditions

  • Opioid Use Disorder

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • STORC — BEHAVIORAL
    STORC will operate as a service model integrating both designated support persons and specialized patient navigators to enhance recovery capital and improve secondary outcomes, including increased OAT retention.

Study Details

We are studying whether training an identified support person and providing patient navigation (i.e. a peer recovery specialist assisting you with finding the right support) after delivery can increase "recovery capital"-the resources that help people with opioid use disorder (OUD) stay in treatment and recover. This study will build upon the research team's prior work in conducting research among pregnant and parenting women with OUD. This project will be directed by the research team at Friends Research Institute in close collaboration with their research and clinical partners at the University of Pennsylvania in Philadelphia, PA. A two-phase study is proposed with an initial 1-year developmental phase (R61) that will develop and pilot test STORC to include support person training. A second 4-year phase (R33) will test STORC in a parallel, two-arm, randomized controlled trial design at two study sites.

Key Dates

First listed
Aug 26, 2026
Start date
Aug 26, 2026
Status verified
Aug 2026
Primary completion
Dec 30, 2026
Completion
Jan 30, 2027

Study Design

Enrollment
10 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE

Arms

  • Experimental: STORC
    STORC is inclusive of patient navigation and support person training.

Primary Outcome Measure

Recruitment Feasibility [ Time Frame: at study completion, up to 3 months ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of PennsylvaniaPhiladelphiaPennsylvania19104
Karen Alexander, PhD
9084510141
Sara Kornfield, PhD
215-746-1255
Sara Kornfield, PhD (PRINCIPAL_INVESTIGATOR)

Find similar trials in Philadelphia, PA

Related Studies